@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP420018.RAnZceYzMTXmsyJMbP6LJ-2BnZxF-TmqxRc0aPuhs3SCk
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP420018.RAnZceYzMTXmsyJMbP6LJ-2BnZxF-TmqxRc0aPuhs3SCk130_head
{
this:
np:hasAssertion
dgn-np:NP420018.RAnZceYzMTXmsyJMbP6LJ-2BnZxF-TmqxRc0aPuhs3SCk130_assertion
;
np:hasProvenance
dgn-np:NP420018.RAnZceYzMTXmsyJMbP6LJ-2BnZxF-TmqxRc0aPuhs3SCk130_provenance
;
np:hasPublicationInfo
dgn-np:NP420018.RAnZceYzMTXmsyJMbP6LJ-2BnZxF-TmqxRc0aPuhs3SCk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP420018.RAnZceYzMTXmsyJMbP6LJ-2BnZxF-TmqxRc0aPuhs3SCk130_assertion
a
np:Assertion
.
dgn-np:NP420018.RAnZceYzMTXmsyJMbP6LJ-2BnZxF-TmqxRc0aPuhs3SCk130_provenance
a
np:Provenance
.
dgn-np:NP420018.RAnZceYzMTXmsyJMbP6LJ-2BnZxF-TmqxRc0aPuhs3SCk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP420018.RAnZceYzMTXmsyJMbP6LJ-2BnZxF-TmqxRc0aPuhs3SCk130_assertion
{
miriam-gene:2637
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGN039ae49c0af70fbb6ba7cace00fcec56
sio:SIO_000628
miriam-gene:2637
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP420018.RAnZceYzMTXmsyJMbP6LJ-2BnZxF-TmqxRc0aPuhs3SCk130_provenance
{
dgn-np:NP420018.RAnZceYzMTXmsyJMbP6LJ-2BnZxF-TmqxRc0aPuhs3SCk130_assertion
dcterms:description
"[Using RT-PCR, we screened members of the EHG family of homeobox genes, comprising EN1 (at 2q14), GBX2 (at 2q36), and EN2, GBX1, and HLXB9 (at 7q36), for dysregulation in acute myeloid leukemia (AML) cell lines indicated by chromosomal breakpoints at these sites.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:15540222
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP420018.RAnZceYzMTXmsyJMbP6LJ-2BnZxF-TmqxRc0aPuhs3SCk130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:44+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetv3.0rdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}